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BOR - Papers in Press, published online ahead of print June 11, 2003.
Biol Reprod 2003, 10.1095/biolreprod.103.016550
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BIOLOGY OF REPRODUCTION 69, 1273–1280 (2003)
DOI: 10.1095/biolreprod.103.016550
© 2003 by the Society for the Study of Reproduction, Inc.


Female Reproductive Tract

Mimicking the Events of Menstruation in the Murine Uterus1

M. Brasted3, C.A. White3, T.G. Kennedy4, and L.A. Salamonsen2,3

Uterine Biology Laboratory,3 Prince Henry's Institute of Medical Research, Clayton, Victoria 3168, Australia Department of Physiology & Pharmacology,4 The University of Western Ontario, London, Ontario, Canada N6A 5C1

Menstruation and endometrial regeneration occur during every normal reproductive cycle in women and some Old World primates. Many of the cellular and molecular events of menstruation have been identified by correlative or in vitro studies, but the lack of a convenient model for menstruation in a laboratory animal has restricted functional studies. In this study, a mouse model for menstruation first described by Finn in the 1980s has been modified for use in a commonly used inbred strain of mouse. A decidual stimulus was applied into the uterine lumen of appropriately primed mice and leukocyte numbers and apoptosis were examined over time following progesterone withdrawal. Endometrial tissue breakdown was initiated after 12–16 h, and by 24 h, the entire decidual zone had been shed. Re-epithelialization was nearly complete by 36 h and the endometrium was fully restored by 48 h. Leukocyte numbers increased significantly in the basal zone by 12 h after progesterone withdrawal, preceding stromal destruction. Stromal apoptosis was detected by TUNEL staining at 0 and 12 h but decreased by 16 h after progesterone withdrawal. This mouse model thus mimics many of the events of human menstruation and has the potential to assist in elucidation of the functional roles of a variety of factors thought to be important in both menstruation and endometrial repair.

1 This work was supported by the NH&MRC of Australia (grants 169003, 143798). T.G.K. contributed to this work while on sabbatical leave from the University of Western Ontario. He was supported in part by a Hudson Hoagland Fellowship.

2 Correspondence: L.A. Salamonsen, Prince Henry's Institute of Medical Research, Level 4, Block E, Monash Medical Centre, 246 Clayton Road, Clayton, Victoria 3168, Australia. FAX: 61 3 9594 6125; lois.salamonsen{at}med.monash.edu.au




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